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Etruscan Shrew Muscle: the Consequences of Being Small Klaus D
The Journal of Experimental Biology 205, 2161–2166 (2002) 2161 Printed in Great Britain © The Company of Biologists Limited 2002 JEB3932 Review Etruscan shrew muscle: the consequences of being small Klaus D. Jürgens* Zentrum Physiologie, Medizinische Hochschule, D-30623 Hannover, Germany *e-mail: [email protected] Accepted 13 May 2002 Summary The skeletal muscles of the smallest mammal, the oxidative metabolism: they have a small diameter, their Etruscan shrew Suncus etruscus, are functionally and citrate synthase activity is higher and their lactate structurally adapted to the requirements of an enormously dehydrogenase activity is lower than in the muscles of any high energy turnover. Isometric twitch contractions of the other mammal and they have a rapid shortening velocity. extensor digitorum longus (EDL) and soleus muscles are Differences in isometric twitch contraction times between shorter than in any other mammal, allowing these muscles different muscles are, at least in part, probably due to to contract at outstandingly high frequencies. The skeletal differences in cytosolic creatine kinase activities. muscles of S. etruscus contract at up to 900 min–1 for respiration, up to 780 min–1 for running and up to 3500 min–1 for shivering. All skeletal muscles investigated Key words: Etruscan shrew, Suncus etruscus, skeletal muscle, lack slow-twitch type I fibres and consist only of fast- extensor digitorum longus, soleus, fibre composition, myosin heavy twitch type IID fibres. These fibres are optimally equipped chain, myosin light chain, lactate dehydrogenase, citrate synthase, with properties enabling a high rate of almost purely creatine kinase, myoglobin, Ca2+ transient, contraction, relaxation. Introduction The Etruscan shrew Suncus etruscus (Savi) and the heart muscle mass, 1.2 % of its body mass (Bartels et al., 1979), bumblebee bat (Craseonycteris thonglongyai), both weighing a value twice as high as expected from allometry, and a heart on average less than 2 g, are the smallest extant mammals. -
Species Examined.Xlsx 8:17 PM 5/31/2011
8:17 PM 5/31/2011 Names Accepted Binomial Name, Family Page Binomial Name, Page Common Name as of 2011, as given in Sperber if different than in Sperber Monotremata 264 Duckbilled Platypus Ornithorhynchus anatinus 264 Marsupialia 266 Slender‐tailed Dunnart Sminthopsis murina 266 Kultarr Antechinomys laniger 268 Gray Four‐eyed Opossum Philander opossum Didelphys opossum 269 (or possibly Virginia Opossum) ( or Didelphis virginiana) Eastern Grey Kangaroo Macropus giganteus 269 Insectivora 272 Elephant Shrew Macroscelides sp. 272 Hedgehog Erinaceus europaeus 273 Eurasian Pygmy Shrew Sorex minutus 274 Eurasian Water Shrew Neomys fodiens 279 Pygmy White Toothed Suncus etruscus Pachyura etrusca 280 (or Etruscan ) Shrew Russian Desman Desmana moschata 280 Chiroptera 281 Greater Flying Fox Pteropus vampyrus Pteropus edulis 281 (Kalong, Kalang) Northern Bat Eptesicus nilssonii Pipistrellus nilssoni 283 Particoloured Bat Vespertilio murinus 285 Xenarthra 287 and Pholidota Armadillos, anteaters and pangolins: Review of the literature only Rodentia 288 European Rabbit Oryctolagus cuniculus 288 Eurasian Red Squirrel Sciurus vulgaris 293 Eurasian Beaver Castor fiber 294 Agile Kangaroo Rats Dipodomys agilis Perodipus agilis 296 Fresno Kangaroo Rat Dipodomys nitratoides exilis Dipodomys meriami exilis 297 Lesser Egyptian Jerboa Jaculus jaculus 298 Field (or Short‐tailed) Vole Microtus agrestis 299 Bank Vole Myodes glareolus Evotomys glareolus 303 European (or Northern) Water Arvicola terrestris 303 Vole Black Rat Rattus Rattus Epimys rattus 303 House Mouse -
World Record World
~ ~ ~ ~ ~ Immerse yourself in the world of super animals! Oldřich Růžička & Tomáš Pernický Pernický Tomáš Oldřich Růžička & ~ ~ The animal world has almost infinite variety. ~ Many of its creatures have strengths similar to superheroes. ~ The world’s fastest animals can move at the speed of a race car; one small creature has the strength of a trained weightlifter; the world’s strongest animal can lift many times its own weight and the longest-lived animal survives for several hundred years. Fastest, world record slowest, strongest, largest, smallest, longest living, furthest jumping, ~ most dangerous, most beautiful, ugliest, deepest diving—these and many other record holders from the animal kingdom fill this book with unexpected, fascinating facts. ~ ����������������AnimalS Oldřich Růžička & Tomáš Pernický ~ The world’s fastest animals Record-breaking flyers/runners/swimmers/jumpers ~ The slowest slowpokes ~ The world’s strongest animals world The largest animals ~ ~ The smallest of the small ~ The most beautiful baby animals Re ~ cord animals cord The ugliest animals on the planet ~ The most dangerous animals Longest-living animals ~ World-record travelers ~ ~ ~ © Designed by B4U Publishing for Albatros, an imprint of Albatros Media Group, 2021. Na Pankráci 30, Prague 4, Czech Republic ~ Printed in China by XY Printing Co., Ltd. Text by Oldřich Růžička, Illustrations by Tomáš Pernický. All rights reserved. $ 14.95 Reproduction of any content is strictly prohibited www.albatrosbooks.com without the written permission of the rights holders. Albatros OSTRICH – Record-breaking The������������� flightless ostrich is the world’s largest living runners THE WORLD’S FASTEST ANIMALS bird and quickest creature on two legs. It lives in � � � � � �� � � � � � � � Africa. -
List of 28 Orders, 129 Families, 598 Genera and 1121 Species in Mammal Images Library 31 December 2013
What the American Society of Mammalogists has in the images library LIST OF 28 ORDERS, 129 FAMILIES, 598 GENERA AND 1121 SPECIES IN MAMMAL IMAGES LIBRARY 31 DECEMBER 2013 AFROSORICIDA (5 genera, 5 species) – golden moles and tenrecs CHRYSOCHLORIDAE - golden moles Chrysospalax villosus - Rough-haired Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus – Lowland Streaked Tenrec 3. Microgale dobsoni - Dobson’s Shrew Tenrec 4. Tenrec ecaudatus – Tailless Tenrec ARTIODACTYLA (83 genera, 142 species) – paraxonic (mostly even-toed) ungulates ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BOVIDAE (46 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Impala 3. Alcelaphus buselaphus - Hartebeest 4. Alcelaphus caama – Red Hartebeest 5. Ammotragus lervia - Barbary Sheep 6. Antidorcas marsupialis - Springbok 7. Antilope cervicapra – Blackbuck 8. Beatragus hunter – Hunter’s Hartebeest 9. Bison bison - American Bison 10. Bison bonasus - European Bison 11. Bos frontalis - Gaur 12. Bos javanicus - Banteng 13. Bos taurus -Auroch 14. Boselaphus tragocamelus - Nilgai 15. Bubalus bubalis - Water Buffalo 16. Bubalus depressicornis - Anoa 17. Bubalus quarlesi - Mountain Anoa 18. Budorcas taxicolor - Takin 19. Capra caucasica - Tur 20. Capra falconeri - Markhor 21. Capra hircus - Goat 22. Capra nubiana – Nubian Ibex 23. Capra pyrenaica – Spanish Ibex 24. Capricornis crispus – Japanese Serow 25. Cephalophus jentinki - Jentink's Duiker 26. Cephalophus natalensis – Red Duiker 1 What the American Society of Mammalogists has in the images library 27. Cephalophus niger – Black Duiker 28. Cephalophus rufilatus – Red-flanked Duiker 29. Cephalophus silvicultor - Yellow-backed Duiker 30. Cephalophus zebra - Zebra Duiker 31. Connochaetes gnou - Black Wildebeest 32. Connochaetes taurinus - Blue Wildebeest 33. Damaliscus korrigum – Topi 34. -
Urotrichus Talpoides)
Molecular phylogeny of a newfound hantavirus in the Japanese shrew mole (Urotrichus talpoides) Satoru Arai*, Satoshi D. Ohdachi†, Mitsuhiko Asakawa‡, Hae Ji Kang§, Gabor Mocz¶, Jiro Arikawaʈ, Nobuhiko Okabe*, and Richard Yanagihara§** *Infectious Disease Surveillance Center, National Institute of Infectious Diseases, Tokyo 162-8640, Japan; †Institute of Low Temperature Science, Hokkaido University, Sapporo 060-0819, Japan; ‡School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu 069-8501, Japan; §John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, HI 96813; ¶Pacific Biosciences Research Center, University of Hawaii at Manoa, Honolulu, HI 96822; and ʈInstitute for Animal Experimentation, Hokkaido University, Sapporo 060-8638, Japan Communicated by Ralph M. Garruto, Binghamton University, Binghamton, NY, September 10, 2008 (received for review August 8, 2008) Recent molecular evidence of genetically distinct hantaviruses in primers based on the TPMV genome, we have targeted the shrews, captured in widely separated geographical regions, cor- discovery of hantaviruses in shrew species from widely separated roborates decades-old reports of hantavirus antigens in shrew geographical regions, including the Chinese mole shrew (Anouro- tissues. Apart from challenging the conventional view that rodents sorex squamipes) from Vietnam (21), Eurasian common shrew are the principal reservoir hosts, the recently identified soricid- (Sorex araneus) from Switzerland (22), northern short-tailed shrew borne hantaviruses raise the possibility that other soricomorphs, (Blarina brevicauda), masked shrew (Sorex cinereus), and dusky notably talpids, similarly harbor hantaviruses. In analyzing RNA shrew (Sorex monticolus) from the United States (23, 24) and Ussuri extracts from lung tissues of the Japanese shrew mole (Urotrichus white-toothed shrew (Crocidura lasiura) from Korea (J.-W. -
Bonner Zoologische Beiträge Band 51 (2002) Heft 4 Seiten 229-254 Bonn, Dezember 2003
© Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zoologicalbulletin.de; www.biologiezentrum.at Bonner zoologische Beiträge Band 51 (2002) Heft 4 Seiten 229-254 Bonn, Dezember 2003 Annotated Checklist of the Mammals of the Republic of Macedonia Boris Krystufek" & Svetozar Petkovski"' "Slovenian Museum of Natural History, Ljubljana, Slovenia -'Macedonian Museum of Natural History, Skopje, Republic of Macedoni Abstract. Eighty-two mammals in 51 genera, 18 families and 6 orders occur in the Republic of Macedonia. Eight species were introduced, either deliberately or accidentally by humans, and the red deer, Cervus elaphus, has been reintroduced. The number of recent human induced extinctions is low, and includes, besides the red deer, also the golden jackal, Canis aureus. Any domesticated mammal has established permanent feral populations. Among the 25 taxa originally named and descri- bed from the Republic of Macedonia, three are currently considered to be valid species: Talpa stankovici, Microtus felteni, and Mus macedonicus. All new names, proposed for Macedonian mammals are listed and type localities are shown on a map. Distribution of 20 species is spot mapped. Key words. Mammalia, status, biogeography, distribution, bibliography INTRODUCTION regions and the lowlands. The first two are delimited by the River Vardar. Western Macedonia is a part of 1.1. General the Sara-Pindus mountain massifs (highest peak 2748 The Republic of Macedonia, one of the top European m), while Eastern Macedonia contains portions of the hot spots of biodiversity (Gaston & Rhian 1994), has Rhodope mountains (highest peak 2252 m). The attracted considerable attention of naturalists in this bedrock is mostly sediments of the Lower Palaeozoic, century. -
1 Checklist of Indian Mammals FINAL.Pmd
CHECKLIST OF INDIAN MAMMALS REVISED AND UPDATED 2008 417 species in 48 families Taxonomy and nomenclature as per Wilson & Reeder (2005) I. ORDER: PROBOSCIDEA 1) Family: Elephantidae (Elephants) 1. Elephas maximus Linnaeus, 1758 Asian Elephant - I, SR, N, BH, BA, M, SE II. ORDER: SIRENIA 2) Family: Dugongidae (Dugong) 2. Dugong dugon (Müller, 1776) Dugong - I, PK(?), SR, M, BA, SE, P, ET, AU - Tropical coastal waters of Indian and W Pacific Ocean III. ORDER: SCANDENTIA 3) Family: Tupaiidae (Treeshrews) 3. Anathana ellioti (Waterhouse, 1850) Madras Treeshrew - I (EN) 4. Tupaia belangeri (Wagner, 1841) Northern Treeshrew - I, N, M, BA, SE, P 5. Tupaia nicobarica (Zelebor, 1869) Nicobar Treeshrew- I (EN) IV. ORDER: PRIMATES SUBORDER: STREPSIRRHINI 4) Family: Lorisidae (Lorises) 6. Loris lydekkerianus Cabrera, 1908 Gray Slender Loris - I, SR 7. Nycticebus bengalensis (Lacépède, 1800) Bengal Slow Loris - I, M, BA, SE, P SUBORDER: HAPLORRHINI 5) Family: Cercopithecidae (Old World monkeys) Subfamily: Cercopithecinae (Macaques) 8. Macaca arctoides (I. Geoffroy, 1831) Stump-tailed Macaque - I, SE, P 9. Macaca assamensis Mc Clelland, 1840 Assam Macaque - I, N, SE, P 10. Macaca fascicularis (Raffles, 1821) Crab-eating Macaque - I, M, SE 11. Macaca leonina (Blyth, 1863) Northern Pig-tailed Macaque - I, M, BA, SE, P 12. Macaca mulatta (Zimmermann, 1780) Rhesus Macaque - I, AF, PK, SE, P 13. Macaca munzala Sinha, Datta, Madhusudan and Mishra, 2005 Arunachal Macaque - I (EN) 14. Macaca radiata (É. Geoffroy, 1812) Bonnet Macaque - I (EN) 15. Macaca silenus (Linnaeus, 1758) Lion-tailed Macaque - I (EN) Subfamily: Colobinae (Langurs and Leaf-monkeys) 16. Semnopithecus ajax (Pocock, 1928) Kashmir Gray Langur - I, PK 17. -
Mammalia, Soricidae) from Vaskapu Cave (N-Hungary
Annales Universitatis Scientiarum Budapestinensis, Sectio Geologica 32,49-56 (1999) Budapest Uppermost Pleistocene shrews (Mammalia, Soricidae) from Vaskapu Cave (N-Hungary) L. Gy. Mészáros' (with 4 figures and 4 tables) Abstract Three shrew species (Sorex araneus LINNAEUS1758, Sorex minutus LlNNAEUS1766 and Sorex alpinus SHINZ1837) were found in the fossiliferous sediments of Vaskapu Cave, near Felsötárkány. The probable stratigraphical position of the sample is Upper Pleistocene, Pilisszántó Horizon (Upper Würm), about 15,000 years B.P. A cold period of the Late Pleistocene with wooded environment is indicated by the soricid assemblage. Introduction Palaeontological excavations were prepared under the leading of Dr. J. HíR in the Lök-völgyi Cave, near Eger in the summer of 1994. The present author was one of the members of the researcher group. Under the preliminary field walks HíR discovered an other fossil locality near the site of the excavations. He identified it as an unexplored part of an old locality, Vaskapu Cave. A sample of about 150 kg was removed from sediments and washed in the field that summer. The sample yielded a rich and well- preserved fossil fauna, containing also 92 shrew bones and teeth. This Soricidae finding is presented in this paper. The Vaskapu "Cave" is a rock shelter, situated about 3.5 km NW of Felsötárkány, by the left side of the panorama road leading from Eger to Miskolc, 350 m above see level. It was originally described as a fossil locality by M. MOTL. She correlated the deposit of the "cave" with the upper part of the Late Pleistocene (MOTL1941). The morphological terms and the measurements (in millimetres) are used after REUMER 1984. -
Tactile Guidance of Prey Capture in Etruscan Shrews
Tactile guidance of prey capture in Etruscan shrews Farzana Anjum*, Hendrik Turni†, Paul G. H. Mulder‡, Johannes van der Burg*, and Michael Brecht*§ *Department of Neuroscience, Erasmus Medical Center, Postbus 1738, 3000 DR, Rotterdam, The Netherlands; †Institute for Behavioral Ecology, Vor dem Kreuzberg 28, 72070 Tu¨bingen, Germany; and ‡Department of Epidemiology and Biostatistics, Erasmus Medical Center, Dr. Molewaterplein 50, 3000 DR, Rotterdam, The Netherlands Edited by Dale Purves, Duke University Medical Center, Durham, NC, and approved September 7, 2006 (received for review July 8, 2006) Whereas visuomotor behaviors and visual object recognition have in this study. Crickets are nocturnal, highly mobile animals been studied in detail, we know relatively little about tactile object endowed with a variety of mechanosensitive organs that mediate representations. We investigate a new model system for the tactile escape behaviors (14). Thus, the behavioral ecology of shrews guidance of behavior, namely prey (cricket) capture by one of the and crickets predestines them to interact by means of sophisti- smallest mammals, the Etruscan shrew, Suncus etruscus. Because cated tactile behaviors. We combined the spatiotemporal anal- of their high metabolic rate and nocturnal lifestyle, Etruscan ysis of numerous attacks with whisker removal and prey manip- shrews are forced to detect, overwhelm, and kill prey in large ulation experiments to answer the following questions: (i) What numbers in darkness. Crickets are exquisitely mechanosensitive, sensory cues are used? (ii) What is the role of the vibrissae? (iii) fast-moving prey, almost as big as the shrew itself. Shrews succeed What is the nature of shrew object representations? in hunting by lateralized, precise, and fast attacks. -
List of Taxa for Which MIL Has Images
LIST OF 27 ORDERS, 163 FAMILIES, 887 GENERA, AND 2064 SPECIES IN MAMMAL IMAGES LIBRARY 31 JULY 2021 AFROSORICIDA (9 genera, 12 species) CHRYSOCHLORIDAE - golden moles 1. Amblysomus hottentotus - Hottentot Golden Mole 2. Chrysospalax villosus - Rough-haired Golden Mole 3. Eremitalpa granti - Grant’s Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus - Lowland Streaked Tenrec 3. Microgale cf. longicaudata - Lesser Long-tailed Shrew Tenrec 4. Microgale cowani - Cowan’s Shrew Tenrec 5. Microgale mergulus - Web-footed Tenrec 6. Nesogale cf. talazaci - Talazac’s Shrew Tenrec 7. Nesogale dobsoni - Dobson’s Shrew Tenrec 8. Setifer setosus - Greater Hedgehog Tenrec 9. Tenrec ecaudatus - Tailless Tenrec ARTIODACTYLA (127 genera, 308 species) ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BALAENIDAE - bowheads and right whales 1. Balaena mysticetus – Bowhead Whale 2. Eubalaena australis - Southern Right Whale 3. Eubalaena glacialis – North Atlantic Right Whale 4. Eubalaena japonica - North Pacific Right Whale BALAENOPTERIDAE -rorqual whales 1. Balaenoptera acutorostrata – Common Minke Whale 2. Balaenoptera borealis - Sei Whale 3. Balaenoptera brydei – Bryde’s Whale 4. Balaenoptera musculus - Blue Whale 5. Balaenoptera physalus - Fin Whale 6. Balaenoptera ricei - Rice’s Whale 7. Eschrichtius robustus - Gray Whale 8. Megaptera novaeangliae - Humpback Whale BOVIDAE (54 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Common Impala 3. Aepyceros petersi - Black-faced Impala 4. Alcelaphus caama - Red Hartebeest 5. Alcelaphus cokii - Kongoni (Coke’s Hartebeest) 6. Alcelaphus lelwel - Lelwel Hartebeest 7. Alcelaphus swaynei - Swayne’s Hartebeest 8. Ammelaphus australis - Southern Lesser Kudu 9. Ammelaphus imberbis - Northern Lesser Kudu 10. Ammodorcas clarkei - Dibatag 11. Ammotragus lervia - Aoudad (Barbary Sheep) 12. -
Checklist of the Central European Mammal Species 6
Checklist of the Central European mammal species 6 Erinaceomorpha Erinaceidae Erinaceus roumanicus Barrett-Hamilton, 1900 – Northern White-breasted Hedgehog Erinaceus europaeus Linnaeus, 1758 – Western European Hedgehog Soricomorpha Soricidae Neomys anomalus Cabrera, 1907 – Miller’s Water Shrew Neomys fodiens (Pennant, 1771) – Eurasian Water Shrew Sorex alpinus Schinz, 1837 – Alpine Shrew Sorex araneus Linnaeus, 1758 – Common Shrew Sorex arunchi Lapini & Testone, 1998 – Udine Shrew Sorex coronatus Millet, 1828 – Crowned Shrew Sorex minutus Linnaeus, 1766 – Eurasian Pygmy Shrew Crocidura leucodon (Hermann, 1780) – Bicoloured white-toothed Shrew Crocidura russula (Hermann, 1780) Greater white-toothed Shrew Crocidura suaveolens (Pallas, 1811) – Lesser white-toothed Shrew Talpidae Talpa europaea Linnaeus, 1758 – Common Mole Chiroptera Rhinolophidae Rhinolophus blasii Peters, 1867 – Blasius’s Horseshoe Bat Rhinolophus euryale Blasius, 1853 – Mediterranean Horseshoe Bat Rhinolophus ferrumequinum (Schreber, 1774) – Greater Horshoe Bat Rhinolophus hipposideros (Bechstein, 1800) – Lesser Horseshoe Bat Rhinolophus mehelyi Matschie, 1901 – Mehely’s Horseshoe Bat Vespertilionidae Eptesicus nilssonii (Keyserling and Blasius, 1839) – Northern Bat Eptesicus serotinus (Schreber, 1774) – Serotine Pipistrellus kuhlii (Kuhl, 1817) – Kuhl’s Pipistrelle Pipistrellus nathusii (Keyserling and Blasius, 1839) – Nathusius’ Pipistrelle Pipistrellus pipistrellus (Schreber, 1774) – Common Pipistrelle Pipistrellus pygmaeus (Leach, 1825) – Soprano Pipistrelle Nyctalus -
HEART and RESPIRATORY RATES in the SMALLEST MAMMAL, the ETRUSCAN SHREW SUNCUS ETRUSCUS (INSECTIVORA : SORICIDAE) K Jurgens, R Fons, T Peters, S Sender
HEART AND RESPIRATORY RATES IN THE SMALLEST MAMMAL, THE ETRUSCAN SHREW SUNCUS ETRUSCUS (INSECTIVORA : SORICIDAE) K Jurgens, R Fons, T Peters, S Sender To cite this version: K Jurgens, R Fons, T Peters, S Sender. HEART AND RESPIRATORY RATES IN THE SMALLEST MAMMAL, THE ETRUSCAN SHREW SUNCUS ETRUSCUS (INSECTIVORA : SORICIDAE). Vie et Milieu / Life & Environment, Observatoire Océanologique - Laboratoire Arago, 1998, pp.105-109. hal-03172845 HAL Id: hal-03172845 https://hal.sorbonne-universite.fr/hal-03172845 Submitted on 18 Mar 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. VIE MILIEU, 1998, 48 (2) : 105-109 HEART AND RESPIRATORY RATES IN THE SMALLEST MAMMAL, THE ETRUSCAN SHREW SUNCUS ETRUSCUS (INSECTIVORA : SORICIDAE) K.D. JURGENS* R. FONS** T. PETERS* S. SENDER* * Zentrum Physiologie, Medizinische Hochschule, D-30623 Hannover, Germany Laboratoire Arago, Université P. et M.-Curie (Paris 6), NRSR URA 2156, 66651 Banyuls-sur-Mer cedex, France HEART RATE ABSTRACT. - Heart and respiratory rates in resting and in stressed Etruscan RESPIRATORY RATE shrews (Suncus etruscus) as well as in animais rewarming from torpor have been OXYGEN TRANSPORT measured in order to investigate the adaptation of the ventilatory and circulatory ELECTROCARDIOGRAM SHREW oxygen transport System of the smallest mammal (average body weight below 2 g) TORPOR to its outstanding weight-specific oxygen consumption rate (270 ml02/(kg min) at Ta = 22 °C).